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acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
adverse drug reaction
alpha glucosidase
alpha-synuclein
anesthesia, general
anterior horn cell disease
aspartate aminotransferase
biologic markers
bionic reconstruction
brachial plexus injury
bradykinesia
calf hypertrophy
cardiomyopathy
children
chromosomal abnormality
complications
congestive heart failure
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
developmental retardation
disability, neurological
dystroglycanopathies
efficacy
Emery-Dreifuss muscular dystrophy
enzyme treatment
enzyme, defect
epidemiology of neurology
gene
gene mutation
gene therapy
genetic neurologic disorders
glycogen storage disease
Gowers maneuver
Guillain Barre syndrome
Guillain Barre syndrome, passive transfer of
hepatomegaly
history of neurology
hypotonia
immunology and the nervous system
L-dopa
Lewy body
life expectancy
lysosomal storage disease
lysosomes, abnoral
molecular genetics
mortality
motor neuron disease
motor system
MRI, abnormal
muscle biopsy
muscle transfer
muscle wasting, diffuse
muscle weakness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myopathy
myopathy, metabolic
myopathy, quadriceps
nerve transfer
neuroleptic, atypical
neurologic disease, diagnoses of
Parkinson disease
Parkinson disease, etiology of
Parkinson disease, nonmotor problems of
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Pompe's disease of glycogen storage
Pompe's disease, infantile
preclinical
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
quality of life
respirator
respiratory failure
respiratory tract infection
review article
rigidity
rippling muscle disease
safety
scoliosis
sinemet
SMN1 gene
spinal muscular atrophy
spinal muscular atrophy, classification
steroid
steroid therapy, CNS treatment and complications with
stimulation, deep brain
storage disease of CNS
survival motor neuron gene
synucleinopathy
systemic illness
toe walking
tongue, enlarged
treatment of neurologic disorder
tremor
weakness
weakness, progressive
weakness, proximal
web sites
Werdnig-Hoffman disease
Showing articles 2650 to 2700 of 3223 << Previous Next >>

Transient Myopathy Apparently Due to Tetracycline
NEJM 307:821-822, Sinclair,D.,et al, 1982

Myopathy Due to Mercaptopropionyl Glycine
BMJ 285:939, Hales,D.S.M.,et al, 1982

Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome
Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
Neurol 32:1311-1314, Pollock,M.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

Electrophysiological & Clinical Correlation in Myasthenia Gravis
Ann Neurol 12:348-354, Oh,S.J.,et al, 1982

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Neurological Aspect of Hyponatraemia
Postgrad Med J 58:737-740, Daggett,P.,et al, 1982

Axillary Nerve Palsy Following Blunt Trauma to the Shoulder Region:A Clinical & Electrophysiological Review
JNNP 45:1027-1032, Berry,H.,et al, 1982

Valproic Acid, Treatment of Myoclonus in Dyssynergia Cerebellaris Myoclonica
Arch Neurol 39:527-528, Sommerville,E.R.,et al, 1982

Carbamazepine for Hemifacial Spasm
Neurol 32:286-287, Alexander,G.E.,et al, 1982

Inclusion Body Myositis Associated With Sjogren's Syndrome
Arch Neurol 39:186-188, Chad,D.,et al, 1982

Sjogren's Syndrome & Polymyositis or Dermatomyositis
Arch Neurol 39:157-163, Ringel,S.P.,et al, 1982

Bregmatic Headache as a Manifestation of Myocardial Ischemia
Arch Neurol 39:130, Lefkowitz,D.,et al, 1982

Fatal CNS Trichinosis
JAMA 247:1024-1025, Gay,T.,et al, 1982

Essential Myoclonus
In Movement Disorder, CD Marsden & S Fahn (Ed) , Butterworth, London, 1982, p 207., , 1982

Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
Pathology 14:435-438, Ojeda,V.J., 1982

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Neurological Complications of Swine Influenza Vaccination
Acat Neurologica Scandinavica 66:413-431, Poser,C.M., 1982

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Sources of Error in the Diagnosis of Guillain-Barre Syndrome
Muscle & Nerve 5:111-117, Feit,H.,et al, 1982

Correlation of CT Scanning and Pathologic Features of Ophthalmic Graves'Disease
Ophthalmol 88:553-564, Trokel,S.L.&Jakobiec,F.A., 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Procainamide-Induced Myasthenia-like Weakness in a Patient with Peripheral Neuropathy
Arch Neurol 38:378-379, Niakan,E.,et al, 1981

Chronic Focal Polymyositis in the Adult
JNNP 44:419-425, Bharucha,N.E.,et al, 1981

Plasmapheresis in Idiopathic Inflammatory Myopathy Experience With 35 Patients
Arch Neurol 38:544-552, Dau,P.C., 1981

Hemifacial Spasm; A Long Term Follow-up of Patients Treated by Posterior Fossa Surgery & Facial Nerve Wrapping
JNNP 44:1100-1103, Kaye,A.H.,et al, 1981

Acute Polymyopathy During Total Parenteral Nutrition
BMJ 283:1578, Stewart,P.M.,et al, 1981

Neurologic Manifestations of Systemic Vasculitis
Am J Med 71:517-524, Moore,P.M.,et al, 1981

Sural Nerve Biopsy in Systemic Necrotizing Vasculitis
Am J Med 71:525-532, Wees,S.J.,et al, 1981

Neurological Manifestation of Accidental Hypothermia
Ann Neurol 10:384-387, Fischbeck,K.H.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Spasticity
et al (Part 1 & 2) NEJM 304:28-33, 96-99., Young,R.R., 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Usefulness of Electrophysiological Studies in the Diagnosis of Lumbosacral Root Disease
Ann Neurol 9:305-308, Tonzola,R.F.,et al, 1981

Diabetic Thoracoabdominal Neuropathy:Clinical & Electrodiagnostic Features
Ann Neurol 9:75-79, Sun,S.F.,et al, 1981

Myoclonus in Down's Syndrome
Arch Neurol 38:453-454, Blumbergs,P.,et al, 1981

Neuroleptic Malignant Syndrome:A Pathogenetic Role for Dopamine Receptor Blockage
Neurol 31:132-137, Henderson,V.W.,et al, 1981

Acute Carbamazepine Toxicity Resulting from Overdose
Neurol 31:621-624, Sullivan,J.B.,et al, 1981

Carotid Endarterectomy:A Prospective Study of Its Efficacy & Safety
Medicine 60:298-309, Allen,G.S.,et al, 1981

Polymyositis & Diffuse Interstitial Lung Disease
Arch Int Med 141:1005-1010, Salmeron,G.,et al, 1981

Polymyositis Beginning as a Focal Process
Arch Neurol 38:439-442, Heffner,R.R.Jr.,et al, 1981

Eosinophilic Myositis, An Unusual Cause of Pseudotumor & Eosinophilia
JAMA 246:70-71, Agrawal,B.L.,et al, 1981

Labetalol-induced Toxic Myopathy
BMJ 282:1824-1825, Teicher,A.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

Myopathy Induced by Rifampicin
BMJ 283:105-106, Jenkins,P.,et al, 1981



Showing articles 2650 to 2700 of 3223 << Previous Next >>